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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1947 1
1948 2
1950 4
1951 5
1952 8
1953 3
1954 7
1955 13
1956 9
1957 8
1958 8
1959 9
1960 9
1961 9
1962 6
1963 8
1964 5
1965 9
1966 10
1967 17
1968 10
1969 17
1970 11
1971 10
1972 16
1973 9
1974 11
1975 17
1976 12
1977 17
1978 16
1979 8
1980 8
1981 12
1982 18
1983 11
1984 13
1985 24
1986 16
1987 29
1988 21
1989 14
1990 23
1991 16
1992 17
1993 23
1994 26
1995 16
1996 21
1997 18
1998 19
1999 15
2000 29
2001 24
2002 14
2003 24
2004 27
2005 17
2006 25
2007 28
2008 31
2009 30
2010 29
2011 27
2012 17
2013 40
2014 29
2015 40
2016 35
2017 38
2018 28
2019 41
2020 31
2021 34
2022 34
2023 7
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1,273 results
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Page 1
Incontinentia Pigmenti.
Cammarata-Scalisi F, Fusco F, Ursini MV. Cammarata-Scalisi F, et al. Actas Dermosifiliogr (Engl Ed). 2019 May;110(4):273-278. doi: 10.1016/j.ad.2018.10.004. Epub 2019 Jan 17. Actas Dermosifiliogr (Engl Ed). 2019. PMID: 30660327 Review. English, Spanish.
Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. ...Approximately 80% of patients have a deletion of exons 4 to 10. Incontinentia pigmenti has an estimated incidence of 0.7 cases per 100,000 births. ...
Incontinentia pigmenti (Bloch-Sulzberger syndrome) is a rare neuroectodermal dysplasia. ...Approximately 80% of patients have …
Incontinentia pigmenti and the eye.
Islam YFK, Khurshid SG. Islam YFK, et al. Curr Opin Ophthalmol. 2022 Nov 1;33(6):525-531. doi: 10.1097/ICU.0000000000000863. Epub 2022 Jul 12. Curr Opin Ophthalmol. 2022. PMID: 35819905 Review.
PURPOSE OF REVIEW: Incontinentia pigmenti (IP) is a rare X-linked dominant phakomatosis that predominately presents with dermatologic manifestations but can also cause central nervous system and ocular abnormalities. ...
PURPOSE OF REVIEW: Incontinentia pigmenti (IP) is a rare X-linked dominant phakomatosis that predominately presents with derma …
Incontinentia Pigmenti: A Summary Review of This Rare Ectodermal Dysplasia With Neurologic Manifestations, Including Treatment Protocols.
Greene-Roethke C. Greene-Roethke C. J Pediatr Health Care. 2017 Nov-Dec;31(6):e45-e52. doi: 10.1016/j.pedhc.2017.07.003. Epub 2017 Sep 1. J Pediatr Health Care. 2017. PMID: 28870493 Review.
Incontinentia pigmenti is a rare neuroectodermal dysplasia caused by a defect in the IKBKG gene (formerly known as NEMO). ...Surveillance protocols for medical management have been established by the Incontinentia Pigmenti International Foundation. Thi …
Incontinentia pigmenti is a rare neuroectodermal dysplasia caused by a defect in the IKBKG gene (formerly known as NEMO). ...S …
Incontinentia pigmenti.
Francis JS, Sybert VP. Francis JS, et al. Semin Cutan Med Surg. 1997 Mar;16(1):54-60. doi: 10.1016/s1085-5629(97)80036-3. Semin Cutan Med Surg. 1997. PMID: 9125766 Review.
This article reviews the clinical features, histopathology, genetics, and differential diagnosis of incontinentia pigmenti. Emphasis is placed on appropriate management strategies for patients with incontinentia pigmenti....
This article reviews the clinical features, histopathology, genetics, and differential diagnosis of incontinentia pigmenti. Em …
Incontinentia pigmenti (Bloch-Sulzberger syndrome).
Narayanan MJ, Rangasamy S, Narayanan V. Narayanan MJ, et al. Handb Clin Neurol. 2015;132:271-80. doi: 10.1016/B978-0-444-62702-5.00020-2. Handb Clin Neurol. 2015. PMID: 26564087 Review.
Incontinentia pigmenti (IP; Bloch-Sulzberger syndrome; OMIM #308300) is an X-linked dominant neurocutaneous disorder with presumed male lethality. ...
Incontinentia pigmenti (IP; Bloch-Sulzberger syndrome; OMIM #308300) is an X-linked dominant neurocutaneous disorder with pres …
Incontinentia pigmenti.
Cohen BA. Cohen BA. Neurol Clin. 1987 Aug;5(3):361-77. Neurol Clin. 1987. PMID: 3306331 Review.
Incontinentia pigmenti (IP) is an unusual genodermatosis occurring almost exclusively in female patients. ...
Incontinentia pigmenti (IP) is an unusual genodermatosis occurring almost exclusively in female patients. ...
Incontinentia pigmenti.
Catalano RA. Catalano RA. Am J Ophthalmol. 1990 Dec 15;110(6):696-700. doi: 10.1016/s0002-9394(14)77070-9. Am J Ophthalmol. 1990. PMID: 2248337 Review. No abstract available.
Incontinentia pigmenti: multisistemic genodermatosis.
Martínez-Gayosso A, García-Romero MT. Martínez-Gayosso A, et al. Bol Med Hosp Infant Mex. 2020;77(3):112-118. doi: 10.24875/BMHIM.19000173. Bol Med Hosp Infant Mex. 2020. PMID: 32496467 English.
Incontinentia pigmenti is an X-linked genodermatosis generally lethal in males; thus, it presents almost exclusively in females. ...Additionally, they are accompanied by neurological abnormalities, such as seizures, and multiple ophthalmological manifestations, such …
Incontinentia pigmenti is an X-linked genodermatosis generally lethal in males; thus, it presents almost exclusively in female …
Incontinentia pigmenti nomenclature.
Sybert VP. Sybert VP. Am J Hum Genet. 1994 Jul;55(1):209-11. Am J Hum Genet. 1994. PMID: 8023849 Free PMC article. Review. No abstract available.
Incontinentia Pigmenti.
Batson R, Keeling BH, Diaz LZ. Batson R, et al. J Pediatr. 2016 Sep;176:218-218.e1. doi: 10.1016/j.jpeds.2016.05.081. Epub 2016 Jun 24. J Pediatr. 2016. PMID: 27349142 No abstract available.
1,273 results